The crucial interplay between metabolic remodeling and the epigenetics could contribute to promote cancer progression. A remarkable association within interaction, LKB1 has been reported, suggesting that the expression of key enzymes involving de novo serine synthesis and DNA methyltransferases like DNMT1 and DNMT3A increase LKB1-deficiency cells. However, the complex interactional link between metabolic remodeling and the epigenetics is still unclear. Hence, we focus on the relationship between YAP/TAZ and serine metabolism to control methylation of DNA or histone in breast cancer with LKB1 deficiency. We hypothesize that YAP/TAZ may have the function to activate key enzymes involving serine metabolism like PSPH and up-regulate the amino acid transporters to supply sources of serine synthesis through activation of C-MYC with TEAD1. Further, we speculate that YAP/TAZ in dependent of FOS may promote DNMT1 and subsequently mediate DNMT1–G9A complex involving serine metabolism and the methylation of DNA and histone. We hope that our study will stimulate further studies and a new targeted therapy and early medical intervention for YAP/TAZ could be a useful option for breast cancer cases complicated with LKB1 deficiency.

Introduction

Recent evidence suggests that the existence of important interplay between metabolic remodeling and the epigenetics such as histone methylation and acetylation can serve as a programmed switch in cancer cell states. Most chromatin-modifying enzymes require substrates or cofactors that are intermediates of cell metabolism, so changes in nutrient availability and utilization can influence epigenetic regulation [1,2]. Whether this interaction generally links to some oncogenic mutations and molecular drivers remains unclear, and this question has implications for understanding tumorigenesis and progression.

LKB1 controls a wide range of cellular functions that include metabolism, proliferation, and cell shape [3], and is mutationally inactivated in a range of sporadic cancers including breast cancer [4,5]. Cancers with low expression of LKB1 tend to exhibit poorer survival and different therapeutic sensitivity from cancers without these [6,7]. LKB1 directly activates AMP-activated protein kinase (AMPK) [8], which is a central regulator of cellular metabolism and energy homeostasis in mammalian tissues [9]. Recently, it demonstrates that significant up-regulation of the DNA methyltransferases DNMT1 and DNMT3A is found in LKB1-deficiency cells [10]. Therefore, the connection between metabolic remodeling and epigenetic regulation is thought to be a driver of tumorigenesis after LKB1 loss.

Serine consumption ranks second only to that of glutamine among the amino acids [11]. Serine can be either obtained from the diet or synthesized de novo from 3-phosphoglycerate (3-PG), an intermediate of glycolysis. Meanwhile, increased serine synthesis [12,13] and up-regulated serine transporter (SLC1A4) [14] has been identified in breast cancer tissues. Cancer cells with LKB1 loss increase the expression of phosphoserine aminotransferase 1 (PSAT1), phosphoserine phosphatase (PSPH) and serine hydroxylmethyltransferase (SHMT1/2) involving de novo serine synthesis pathway (SSP) in breast cancer [10]. In addition, the amplification of phosphoglycerate dehydrogenase (PHGDH), the first enzyme of the SSP and catalyze the conversion of 3-PG to 3-phosphohydroxypyruvate (3-PH), also occurs in some breast cancers. Cancer cells that support one-carbon unit demand by up-regulation of serine synthesis can do so via increased SSP genes expression. Moreover, a key regulator of SSP gene is ATF4 [15], a member of the basic region leucine zipper (bZIP) transcription factor family that can regulate gene transcription by forming a homodimer or heterodimer with other bZIP transcription factors and respond to stresses, such as amino acid deprivation [16]. ATF4 regulated by mechanistic target of rapamycin complex I (mTORC1) activation directly binds and activates the promoters of PHGDH, PSAT1, and SHMT2 [17]. Simultaneously, activated TORC1 promotes one-carbon metabolism for nucleotide synthesis by independently inducing ATF4-mediated SSP genes expression [18]. Besides, cells with LKB1 knockdown showed reduced activity of AMPK and subsequent activation of mTORC1 [10]. Therefore, the effects of serine metabolism on epigenetic regulation may be modulated by LKB1/mTORC1/ATF4 pathway.

Glutamine plays a predominant role in serine synthetic process, which provides nitrogen into a transamination reaction and produces α-ketoglutarate (α-KG) catalyzed by PSAT1. It has been shown that silencing LKB1 is sufficient to promote glutaminolysis and increase glutamine metabolism to fuel cell growth and lipid biosynthesis, which is mediated by the transcription factor HIF-1α that displays increased protein stabilization under normoxia when LKB1 is deleted [19]. Meanwhile, Yes-associated protein-1 (YAP1) directly enhances glutamine synthetase (GLUL) expression and activity, elevating steady-state levels of glutamine and enhancing the relative enrichment of nitrogen [20]. In addition, it demonstrates that YAP1 directly enhances GLUL expression and activity, and up-regulated expression of SLC38A1 and SLC7A5, main glutamine transporters [2022]. Together, we speculate that YAP1 may increase glutamine level and enrich nitrogen to elevate synthesizing level of serine by enhancing GLUL expression and activity, elevating glutamine uptake, and enhancing the relative enrichment of nitrogen when LKB1 is silenced.

YAP and transcriptional co-activator with PDZ-binding motif (TAZ) are the major downstream effectors of the Hippo pathway, which was recently found to be regulated by metabolic pathways such as aerobic glycolysis [23]. Interestingly, YAP is activated and have significant implications in LKB1-deficiency human malignancies, mechanism of which depends on MARK/Scribble and is dependent on AMPK or mTORC1 [24]. Besides, ATF4 promotes the stabilization of the large tumor suppressor 1 (LATS1) under oxidative stress that inactivates YAP by phosphorylation [25] and specifically binds to the YAP promoter in HepG2 cells to enhance the transcriptional level of YAP [26]. Meanwhile, these reports indicate that YAP/TAZ may mediate up-regulation of key enzymes in SSP for one-carbon metabolism and tumor growth. As for serine metabolism, there is also evidence showing that TAZ S89A induces expression of the serine biosynthesis pathway (PHGDH, PASAT1, and PSPH) in C2C12 cells [27]. In addition, serine can be mainly synthesized from glucose and glycine and there is an evidence that YAP1 was found to positively regulate C-MYC and glucose transport-1 (GLUT1) mRNA levels in complex with TEAD1 [28] and it reports that activation of C-MYC also leads to elevate glutathione (GSH) production and drives PSPH to promote serine biosynthesis [29]. Thus, YAP/TAZ may be activated in LKB1-deficiency human malignancies depending on ATF4 up-regulation and increase serine synthesis through up-regulating key enzymes and supplying synthetic sources such as glucose.

We also analyzed the correlation between TAZ or YAP1 mRNA expression and LKB1 mRNA levels as well as the relevance between TAZ or YAP1 mRNA expression and PHGDH mRNA levels in the breast cancer dataset from The Cancer Genome Atlas (TCGA 2012). In accordance with the observations, we find that the expression of TAZ or YAP1 and LKB1 are negatively correlated (P<0.0001), but there are positive correlations between TAZ or YAP1 expression and PHGDH level (P<0.0001) (Figure 1).

Correlation analysis for TAZ or YAP1 mRNA expression and LKB1 mRNA levels as well as TAZ or YAP1 mRNA expression and PHGDH mRNA levels in breast cancer tissues

Figure 1
Correlation analysis for TAZ or YAP1 mRNA expression and LKB1 mRNA levels as well as TAZ or YAP1 mRNA expression and PHGDH mRNA levels in breast cancer tissues

(A) After annotating the gene microarrays according to the TCGA 2012, we identify the expression levels of YAP1 were negative correlated with LKB1 level (P<0.0001). (B) The expression of TAZ and LKB1 in breast cancer tissues includes negative correlation (P<0.0001). (C) There is a positive correlation between the levels of YAP1 and the expression of PHGDH in breast cancer (P<0.0001). (D) The data from TCGA breast cancer suggest a positive correlation in TAZ expression compared with PHGDH level.

Figure 1
Correlation analysis for TAZ or YAP1 mRNA expression and LKB1 mRNA levels as well as TAZ or YAP1 mRNA expression and PHGDH mRNA levels in breast cancer tissues

(A) After annotating the gene microarrays according to the TCGA 2012, we identify the expression levels of YAP1 were negative correlated with LKB1 level (P<0.0001). (B) The expression of TAZ and LKB1 in breast cancer tissues includes negative correlation (P<0.0001). (C) There is a positive correlation between the levels of YAP1 and the expression of PHGDH in breast cancer (P<0.0001). (D) The data from TCGA breast cancer suggest a positive correlation in TAZ expression compared with PHGDH level.

Methyltransferases and demethylases have a central role in regulation of transcription by controlling the methylation state of histone and DNA. S-adenosylmethionine (SAM) as the methyl group donor primarily derives from serine-driven one-carbon metabolism [30]. It recently identifies a G9A-dependent epigenetic mechanism for transcriptional activation of the serine pathway in cancer [31]. G9A, also known as EHMT2 and KMT1C, is a H3K9 methyltransferase that has a primary role in catalyzing H3K9me1 and H3K9me2 in euchromatin [32], with H3K9me1 being associated with active chromatin and H3K9me2 being a repressive mark [33,34]. Moreover, higher G9A expression significantly increases serine and glycine biosynthesis in the cell depending on up-regulation of ATF4 [31]. Multiple histone lysine demethylases (KDMs) catalyze the removal of methyl groups at H3K9: KDM3B can remove all methyl groups (me 1–3); KDM4 only me2 and me3; and KDM3A and KDM7A-B only me1 and me2 [34,33]. Thus, the KDM4C requires ATF4 for the transcriptionally control of amino acid including serine biosynthesis and transport by removing the repressive marks H3K9me2 and H3K9me3 at their loci [35]. As for DNMTs, it confirms that DNMT1 interacts with ATF4, FOS, and FOSB and is activated [36]. Meanwhile, DNMT1 as the primary loading factor is shown to directly bind G9a both in vivo and in vitro and to colocalize with dimethylated H3K9 (H3K9me2) at replication foci [37]. And YAP1 converges on the transcription factor FOS and activates a transcriptional program [38], which may include DNMT1. Simultaneously, Yorkie (YAP homologs) can activate transcription by recruiting NcoA6, a subunit of Trithorax-related (Trr)-methyltransferase complexes, which links the control of cell proliferation by Hippo signaling to epigenetic modification [39]. It has also demonstrated that Set7, a SET-domain-containing lysine methyltransferase, could monomethylate Yap at K494 and maintain cytoplasmic localization [40]. Therefore, there is a complex interrelationship between methylation regulation of DNA or nonhistone proteins and function of YAP, which should be further established.

Consequences of the hypothesis and discussion

In summary, for breast cancer cells with LKB1-deficient, YAP/TAZ is up-regulated while key enzymes involving serine metabolism and methylation-regulation are activated. Further, high expression of TAZ S89A could directly promote the expression of key enzymes involving serine metabolism, and YAP/TAZ modulates up-regulation of the amino acid transporters (SLC38A1, SLC7A5, and SLC3A2) and GLUT1 to supply sources of serine synthesis through activation of C-MYC with TEAD1. Subsequently, ATF4 that is reported to modulate the serine metabolism could specifically bind to the Yap promoter to enhance the transcriptional level of YAP. In addition, the methylation of DNA and histone involving in this process is not unambiguously elucidated, and some transmethylases like G9A and DNMTs and demethyltransferases like KDM4C might participate in the regulation. Hence, we hypothesize that YAP/TAZ may have the function to link serine metabolism to methylation in a subset of breast cancer patients with LKB1 deficient (Figure 2). Further, we speculate that YAP/TAZ in dependent or independent manner of ATF4 promote key enzymes and transporters involving serine metabolism and the methylation of DNA and histone.

Working model for YAP/TAZ-mediated activation of serine metabolism and methylation regulation in LKB1-deficient breast cancer progression

Figure 2
Working model for YAP/TAZ-mediated activation of serine metabolism and methylation regulation in LKB1-deficient breast cancer progression

Working model for YAP/TAZ-mediated activation of serine metabolism and methylation regulation in LKB1-deficient breast cancer progression.

Figure 2
Working model for YAP/TAZ-mediated activation of serine metabolism and methylation regulation in LKB1-deficient breast cancer progression

Working model for YAP/TAZ-mediated activation of serine metabolism and methylation regulation in LKB1-deficient breast cancer progression.

Our hypothesis points to the role of YAP/TAZ in the regulation of serine metabolism and histone methylation in a subset of breast cancer patients with LKB1 deficient. The presence of YAP/TAZ overexpression in breast cancer cases complicated with LKB1 deficient could worsen survival and contribute to cancer progression. If our hypothesis is confirmed by further studies, a new targeted therapy and early medical intervention for YAP/TAZ could be a useful option for a subgroup of breast cancer cases complicated with LKB1 deficient, which may have important clinical and health implication.

Funding

This work was partially supported by a NSFC grant to Prof. Shengrong Sun [grant number 81471781] and a NSFC grant to Dr Juanjuan Li [grant number 81302314]. The authors thank Yimin Zhang for assistance in improving the quality of language.

Competing Interests

The authors declare that there are no competing interests associated with the manuscript.

Abbreviations

     
  • α-KG

    α-ketoglutarate

  •  
  • 3-PG

    3-phosphoglycerate

  •  
  • 3-PH

    3-phosphohydroxypyruvate

  •  
  • AMPK

    AMP-activated protein kinase

  •  
  • bZIP

    basic region leucine zipper

  •  
  • GLUL

    glutamine synthetase

  •  
  • GLUT1

    glucose transport-1

  •  
  • GSH

    glutathione

  •  
  • LATS1

    large tumor suppressor 1

  •  
  • PHGDH

    phosphoglycerate dehydrogenase

  •  
  • PSAT1

    phosphoserine aminotransferase 1

  •  
  • PSPH

    phosphoserine phosphatase

  •  
  • SHMT1/2

    serine hydroxylmethyltransferase

  •  
  • SSP

    serine synthesis pathway

References

References
1
Su
X.
,
Wellen
K.E.
and
Rabinowitz
J.D.
(
2016
)
Metabolic control of methylation and acetylation
.
Curr. Opin. Chem. Biol.
30
,
52
60
2
Kinnaird
A.
,
Zhao
S.
,
Wellen
K.E.
and
Michelakis
E.D.
(
2016
)
Metabolic control of epigenetics in cancer
.
Nat. Rev. Cancer
11
,
694
707
3
Hezel
A.F.
and
Bardeesy
N.
(
2008
)
LKB1; linking cell structure and tumor suppression
.
Oncogene
55
,
6908
6919
4
Rhodes
L.V.
,
Tate
C.R.
,
Hoang
V.T.
,
Burks
H.E.
,
Gilliam
D.
,
Martin
E.C.
et al
(
2015
)
Regulation of triple-negative breast cancer cell metastasis by the tumor-suppressor liver kinase B1
.
Oncogenesis
e168
5
Chen
I.C.
,
Chang
Y.C.
,
Lu
Y.S.
,
Chung
K.P.
,
Huang
C.S.
,
Lu
T.P.
et al
(
2016
)
Clinical relevance of liver kinase B1(LKB1) protein and gene expression in breast cancer
.
Sci. Rep.
21374
6
Liu
W.
,
Monahan
K.B.
,
Pfefferle
A.D.
,
Shimamura
T.
,
Sorrentino
J.
,
Chan
K.T.
et al
(
2012
)
LKB1/STK11 inactivation leads to expansion of a prometastatic tumor subpopulation in melanoma
.
Cancer Cell
6
,
751
764
7
Chen
Z.
,
Cheng
K.
,
Walton
Z.
,
Wang
Y.
,
Ebi
H.
,
Shimamura
T.
et al
(
2012
)
A murine lung cancer co-clinical trial identifies genetic modifiers of therapeutic response
.
Nature
7391
,
613
617
8
Woods
A.
,
Johnstone
S.R.
,
Dickerson
K.
,
Leiper
F.C.
,
Fryer
L.G.
,
Neumann
D.
et al
(
2003
)
LKB1 is the upstream kinase in the AMP-activated protein kinase cascade
.
Curr. Biol.
22
,
2004
2008
9
Faubert
B.
,
Vincent
E.E.
,
Poffenberger
M.C.
and
Jones
R.G.
(
2015
)
The AMP-activated protein kinase (AMPK) and cancer: many faces of a metabolic regulator
.
Cancer Lett.
2
,
165
170
10
Kottakis
F.
,
Nicolay
B.N.
,
Roumane
A.
,
Karnik
R.
,
Gu
H.
,
Nagle
J.M.
et al
(
2016
)
LKB1 loss links serine metabolism to DNA methylation and tumorigenesis
.
Nature
7629
,
390
395
11
Jain
M.
,
Nilsson
R.
,
Sharma
S.
,
Madhusudhan
N.
,
Kitami
T.
,
Souza
A.L.
et al
(
2012
)
Metabolite profiling identifies a key role for glycine in rapid cancer cell proliferation
.
Science
6084
,
1040
1044
12
Kim
H.Y.
,
Lee
K.M.
,
Kim
S.H.
,
Kwon
Y.J.
,
Chun
Y.J.
and
Choi
H.K.
(
2016
)
Comparative metabolic and lipidomic profiling of human breast cancer cells with different metastatic potentials
.
Oncotarget
7
,
67111
67128
13
Possemato
R.
,
Marks
K.M.
,
Shaul
Y.D.
,
Pacold
M.E.
,
Kim
D.
,
Birsoy
K.
et al
(
2011
)
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer
.
Nature
7360
,
346
350
14
Pollari
S.
,
Kakonen
S.M.
,
Edgren
H.
,
Wolf
M.
,
Kohonen
P.
,
Sara
H.
et al
(
2011
)
Enhanced serine production by bone metastatic breast cancer cells stimulates osteoclastogenesis
.
Breast Cancer Res. Treat.
2
,
421
430
15
Ye
J.
,
Mancuso
A.
,
Tong
X.
,
Ward
P.S.
,
Fan
J.
,
Rabinowitz
J.D.
et al
(
2012
)
Pyruvate kinase M2 promotes de novo serine synthesis to sustain mTORC1 activity and cell proliferation
.
Proc. Natl. Acad. Sci. U.S.A.
18
,
6904
6909
16
Ameri
K.
and
Harris
A.L.
(
2008
)
Activating transcription factor 4
.
Int. J. Biochem. Cell Biol.
1
,
14
21
17
DeNicola
G.M.
,
Chen
P.H.
,
Mullarky
E.
,
Sudderth
J.A.
,
Hu
Z.
,
Wu
D.
et al
(
2015
)
NRF2 regulates serine biosynthesis in non-small cell lung cancer
.
Nat. Genet.
12
,
1475
1481
18
Ben-Sahra
I.
,
Hoxhaj
G.
,
Ricoult
S.J.
,
Asara
J.M.
and
Manning
B.D.
(
2016
)
mTORC1 induces purine synthesis through control of the mitochondrial tetrahydrofolate cycle
.
Science
6274
,
728
733
19
Faubert
B.
,
Vincent
E.E.
,
Griss
T.
,
Samborska
B.
,
Izreig
S.
,
Svensson
R.U.
et al
(
2014
)
Loss of the tumor suppressor LKB1 promotes metabolic reprogramming of cancer cells via HIF-1alpha
.
Proc. Natl. Acad. Sci. U.S.A.
7
,
2554
2559
20
Cox
A.G.
,
Hwang
K.L.
,
Brown
K.K.
,
Evason
K.J.
,
Beltz
S.
,
Tsomides
A.
et al
(
2016
)
Yap reprograms glutamine metabolism to increase nucleotide biosynthesis and enable liver growth
.
Nat. Cell Biol.
8
,
886
896
21
Hansen
C.G.
,
Ng
Y.L.
,
Lam
W.L.
,
Plouffe
S.W.
and
Guan
K.L.
(
2015
)
The Hippo pathway effectors YAP and TAZ promote cell growth by modulating amino acid signaling to mTORC1
.
Cell Res.
12
,
1299
1313
22
Park
Y.Y.
,
Sohn
B.H.
,
Johnson
R.L.
,
Kang
M.H.
,
Kim
S.B.
,
Shim
J.J.
et al
(
2016
)
Yes-associated protein 1 and transcriptional coactivator with PDZ-binding motif activate the mammalian target of rapamycin complex 1 pathway by regulating amino acid transporters in hepatocellular carcinoma
.
Hepatology
1
,
159
172
23
Santinon
G.
,
Pocaterra
A.
and
Dupont
S.
(
2016
)
Control of YAP/TAZ Activity by Metabolic and Nutrient-Sensing Pathways
.
Trends Cell Biol.
4
,
289
299
24
Mohseni
M.
,
Sun
J.
,
Lau
A.
,
Curtis
S.
,
Goldsmith
J.
,
Fox
V.L.
et al
(
2014
)
A genetic screen identifies an LKB1-MARK signalling axis controlling the Hippo-YAP pathway
.
Nat. Cell Biol.
1
,
108
117
25
Rajesh
K.
,
Krishnamoorthy
J.
,
Gupta
J.
,
Kazimierczak
U.
,
Papadakis
A.I.
,
Deng
Z.
et al
(
2016
)
The eIF2alpha serine 51 phosphorylation-ATF4 arm promotes HIPPO signaling and cell death under oxidative stress
.
Oncotarget
32
,
51044
51058
26
Wu
H.
,
Wei
L.
,
Fan
F.
,
Ji
S.
,
Zhang
S.
,
Geng
J.
et al
(
2015
)
Integration of Hippo signalling and the unfolded protein response to restrain liver overgrowth and tumorigenesis
.
Nat. Commun.
6239
27
Mohamed
A.
,
Sun
C.
,
De Mello
V.
,
Selfe
J.
,
Missiaglia
E.
,
Shipley
J.
et al
(
2016
)
The Hippo effector TAZ (WWTR1) transforms myoblasts and TAZ abundance is associated with reduced survival in embryonal rhabdomyosarcoma
.
J. Pathol.
1
,
3
14
28
Valis
K.
,
Talacko
P.
,
Grobarova
V.
,
Cerny
J.
and
Novak
P.
(
2016
)
Shikonin regulates C-MYC and GLUT1 expression through the MST1-YAP1-TEAD1 axis
.
Exp. Cell Res.
2
,
273
281
29
Sun
L.
,
Song
L.
,
Wan
Q.
,
Wu
G.
,
Li
X.
,
Wang
Y.
et al
(
2015
)
cMyc-mediated activation of serine biosynthesis pathway is critical for cancer progression under nutrient deprivation conditions
.
Cell Res.
4
,
429
444
30
Fan
J.
,
Ye
J.
,
Kamphorst
J.J.
,
Shlomi
T.
,
Thompson
C.B.
and
Rabinowitz
J.D.
(
2014
)
Quantitative flux analysis reveals folate-dependent NADPH production
.
Nature
7504
,
298
302
31
Ding
J.
,
Li
T.
,
Wang
X.
,
Zhao
E.
,
Choi
J.H.
,
Yang
L.
et al
(
2013
)
The histone H3 methyltransferase G9A epigenetically activates the serine-glycine synthesis pathway to sustain cancer cell survival and proliferation
.
Cell Metab.
6
,
896
907
32
Shinkai
Y.
and
Tachibana
M.
(
2011
)
H3K9 methyltransferase G9a and the related molecule GLP
.
Genes. Dev.
8
,
781
788
33
Mosammaparast
N.
and
Shi
Y.
(
2010
)
Reversal of histone methylation: biochemical and molecular mechanisms of histone demethylases
.
Annu. Rev. Biochem.
155
179
34
Black
J.C.
,
Van Rechem
C.
and
Whetstine
J.R.
(
2012
)
Histone lysine methylation dynamics: establishment, regulation, and biological impact
.
Mol. Cell
4
,
491
507
35
Zhao
E.
,
Ding
J.
,
Xia
Y.
,
Liu
M.
,
Ye
B.
,
Choi
J.H.
et al
(
2016
)
KDM4C and ATF4 cooperate in transcriptional control of amino acid metabolism
.
Cell Rep.
3
,
506
519
36
Hervouet
E.
,
Vallette
F.M.
and
Cartron
P.F.
(
2010
)
Dnmt1/Transcription factor interactions: an alternative mechanism of DNA methylation inheritance
.
Genes. Cancer
5
,
434
443
37
Esteve
P.O.
,
Chin
H.G.
,
Smallwood
A.
,
Feehery
G.R.
,
Gangisetty
O.
,
Karpf
A.R.
et al
(
2006
)
Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication
.
Genes Dev.
22
,
3089
3103
38
Shao
D.D.
,
Xue
W.
,
Krall
E.B.
,
Bhutkar
A.
,
Piccioni
F.
,
Wang
X.
et al
(
2014
)
KRAS and YAP1 converge to regulate EMT and tumor survival
.
Cell
1
,
171
184
39
Oh
H.
,
Slattery
M.
,
Ma
L.
,
White
K.P.
,
Mann
R.S.
and
Irvine
K.D.
(
2014
)
Yorkie promotes transcription by recruiting a histone methyltransferase complex
.
Cell Rep.
2
,
449
459
40
Oudhoff
M.J.
,
Freeman
S.A.
,
Couzens
A.L.
,
Antignano
F.
,
Kuznetsova
E.
,
Min
P.H.
et al
(
2013
)
Control of the hippo pathway by Set7-dependent methylation of Yap
.
Dev. Cell
2
,
188
194
This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).